Join Our Quality Team: Hiring for QA & DQA Professionals (Executive/Sr. Executive)
About the Company:
A leading pharmaceutical company committed to delivering high-quality healthcare products, we operate state-of-the-art facilities and uphold the highest standards of quality and compliance. We are seeking dedicated and experienced professionals to strengthen our Quality Assurance team at our Haridwar facility.
About the Opportunity:
We are actively looking for dynamic and skilled individuals to fill Executive and Senior Executive roles within our Quality Assurance (QA) and Documentation Quality Assurance (DQA) departments. If you possess a strong understanding of pharmaceutical quality systems and are ready to contribute to a culture of excellence, we encourage you to explore these exciting opportunities.
Open Positions:
1. Quality Assurance (QA) – Executive / Sr. Executive
- Experience: 2 to 6 years of relevant experience within a pharmaceutical manufacturing environment.
- Qualification: Bachelor of Pharmacy (B. Pharma), Master of Pharmacy (M. Pharma), or Master of Science (M.Sc.).
- Key Responsibilities:
- Conducting sampling procedures for Raw Materials (RM), Packing Materials (PM), Semi-Finished Goods (SFG), and Finished Goods (FG).
- Performing In-Process Quality Assurance (IPQA) checks across manufacturing and packing lines.
- Managing and reviewing Quality Management System (QMS) documents, including deviations, incidents, and change controls.
- Overseeing dispensing operations and ensuring strict adherence to standard operating procedures.
- Executing line clearance activities to prepare for new batches or products.
2. Documentation Quality Assurance (DQA) – Executive / Sr. Executive
- Experience: 2 to 6 years of experience, preferably in a documentation or quality assurance role within the pharmaceutical sector.
- Qualification: Bachelor of Pharmacy (B. Pharma), Master of Pharmacy (M. Pharma), or Master of Science (M.Sc.).
- Key Responsibilities:
- Thorough review of Batch Production Records (BPRs) and associated documentation.
- Managing and reviewing QMS documents such as deviations, incidents, change controls, and Corrective and Preventive Actions (CAPA).
- Preparation and review of Annual Product Quality Review (APQR) reports.
- Ensuring robust data integrity across all pharmaceutical documentation.
- Reviewing Qualification and Validation documents, including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Work Location: Haridwar
Candidate Profile:
We strongly prefer candidates with prior working experience in regulated pharmaceutical plants that are approved by international regulatory bodies such as USFDA, EUGMP, MHRA, TGA, or WHO. Your experience in such environments will be a significant asset.
Walk-in Interview Details:
- Date: 26th July 2026
- Time: 9:00 AM to 5:00 PM
- Venue: Morepen Laboratories Ltd., Baddi
What to Bring:
Candidates attending the interview are requested to bring the following documents:
- An updated Curriculum Vitae (CV)
- Your latest passport-size photograph
- Salary slips for the last three months
- A valid Aadhar Card
Join our dedicated team and contribute to our unwavering commitment to pharmaceutical quality and patient safety!
